Evidence map›Paper›PMID 31953186›Full record

ArticleJournal of the American Academy of Child and Adolescent Psychiatry2021

Identifying Adolescents at Risk for Depression: A Prediction Score Performance in Cohorts Based in 3 Different Continents.

Thiago Botter-Maio Rocha, Helen L Fisher, Arthur Caye, Luciana Anselmi, Louise Arseneault, Fernando C Barros, Avshalom Caspi, Andrea Danese, Helen Gonçalves, Hona Lee Harrington and 8 more

Abstract read
In one paragraph

Article in Journal of the American Academy of Child and Adolescent Psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 3 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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  15. A prognostic model for predicting functional impairment in youth mental health services.European psychiatry : the journal of the Association of European Psychiatrists · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Thiago Botter-Maio RochaSchool of Medicine, Universidade Federal do Rio Grande do Sul, Brazil; Division of Child & Adolescent Psychiatry, Hospital de Clínicas de Porto Alegre, Brazil.
Helen L FisherSocial, Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, United Kingdom.
Arthur CayeSchool of Medicine, Universidade Federal do Rio Grande do Sul, Brazil.
Luciana AnselmiPostgraduate Program in Epidemiology, Universidade Federal de Pelotas, Pelotas, Brazil.
Louise ArseneaultSocial, Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, United Kingdom.
Fernando C BarrosPostgraduate Program in Epidemiology, Universidade Federal de Pelotas, Pelotas, Brazil.
Avshalom CaspiSocial, Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, United Kingdom; Duke University, Durham, North Carolina.
Andrea DaneseSocial, Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, United Kingdom; National and Specialist CAMHS Clinic for Trauma, Anxiety, and Depression, South London and Maudsley NHS Foundation Trust, London, United Kingdom; Institute of Psychiatry, Psychology & Neuroscience, King's College London, United Kingdom.
Helen GonçalvesPostgraduate Program in Epidemiology, Universidade Federal de Pelotas, Pelotas, Brazil.
Hona Lee HarringtonDuke University, Durham, North Carolina.
Renate HoutsDuke University, Durham, North Carolina.
Ana M B MenezesPostgraduate Program in Epidemiology, Universidade Federal de Pelotas, Pelotas, Brazil.
Terrie E MoffittSocial, Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, United Kingdom; Duke University, Durham, North Carolina.
Valeria MondelliInstitute of Psychiatry, Psychology & Neuroscience, King's College London, United Kingdom; National Institute for Health Research (NIHR) Maudsley Biomedical Research Centre, South London and Maudsley NHS Foundation Trust, London, United Kingdom.
Richie PoultonDunedin Multidisciplinary Health and Development Research Unit, University of Otago, Dunedin, New Zealand.
Luis Augusto RohdeSchool of Medicine, Universidade Federal do Rio Grande do Sul, Brazil; Division of Child & Adolescent Psychiatry, Hospital de Clínicas de Porto Alegre, Brazil; National Institute of Developmental Psychiatry for Children and Adolescents, São Paulo, Brazil.
Fernando WehrmeisterPostgraduate Program in Epidemiology, Universidade Federal de Pelotas, Pelotas, Brazil.
Christian KielingSchool of Medicine, Universidade Federal do Rio Grande do Sul, Brazil; Division of Child & Adolescent Psychiatry, Hospital de Clínicas de Porto Alegre, Brazil. Electronic address: ckieling@ufrgs.br.

Funding

Is mental disorder a preventable cause of age-related disease? The Dunedin Study.R01AG032282 · NIA · DUKE UNIVERSITY · PI CASPI, AVSHALOM, MOFFITT, TERRIE E · 2009 to 2025
$9.5M
Science CoreP2CHD065563 · NICHD · DUKE UNIVERSITY · PI James Moody · 2015 to 2026
$5.7M
Neuropsychological and genomic signatures of violence exposure in childhoodR01HD077482 · NICHD · DUKE UNIVERSITY · PI CASPI, AVSHALOM · 2013 to 2018
$2.8M
Medical Research Council G1002190Medical Research Council MC_PC_MR/R019460/1Medical Research Council MR/P005918/1NIA NIH HHS R01 AG032282NICHD NIH HHS P2C HD065563NICHD NIH HHS R01 HD077482Wellcome Trust
6 · The paper itself

Abstract

objectivePrediction models have become frequent in the medical literature, but most published studies are conducted in a single setting. Heterogeneity between development and validation samples has been posited as a major obstacle for the generalization of models. We aimed to develop a multivariable prognostic model using sociodemographic variables easily obtainable from adolescents at age 15 to predict a depressive disorder diagnosis at age 18 and to evaluate its generalizability in 2 samples from diverse socioeconomic and cultural settings.

methodData from the 1993 Pelotas Birth Cohort were used to develop the prediction model, and its generalizability was evaluated in 2 representative cohort studies: the Environmental Risk (E-Risk) Longitudinal Twin Study and the Dunedin Multidisciplinary Health and Development Study.

resultsAt age 15, 2,192 adolescents with no evidence of current or previous depression were included (44.6% male). The apparent C-statistic of the models derived in Pelotas ranged from 0.76 to 0.79, and the model obtained from a penalized logistic regression was selected for subsequent external evaluation. Major discrepancies between the samples were identified, impacting the external prognostic performance of the model (Dunedin and E-Risk C-statistics of 0.63 and 0.59, respectively). The implementation of recommended strategies to account for this heterogeneity among samples improved the model's calibration in both samples.

conclusionAn adolescent depression risk score comprising easily obtainable predictors was developed with good prognostic performance in a Brazilian sample. Heterogeneity among settings was not trivial, but strategies to deal with sample diversity were identified as pivotal for providing better risk stratification across samples. Future efforts should focus on developing better methodological approaches for incorporating heterogeneity in prognostic research.

Indexed as

DepressionAdolescentBrazilCohort StudiesFemaleHumansLongitudinal StudiesMalePrognosisadolescentcohort studiesdepressionprognosisrisk assessment

Identifiers

PMID31953186
PMCPMC8215370

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.